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ACTIVE NOT RECRUITING Phase 4

Effectiveness of Deep Brain Stimulation for Treating People With Treatment Resistant Obsessive-Compulsive Disorder

NCT00640133 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the safety and effectiveness of deep brain stimulation in treating people with severe and otherwise treatment-resistant obsessive-compulsive disorder.

Interventions

  • DEVICE Sham DBS
  • DEVICE Active DBS

Study Locations (9)

California

  • Kaiser Permanente Redwood City Hospital — Redwood City

District of Columbia

  • George Washington University Hospital — Washington D.C.

Florida

  • University of Florida — Gainesville

Illinois

  • University of Chicago — Chicago

Massachusetts

  • Massachusetts General Hospital — Boston

Minnesota

  • Mayo Clinic — Rochester

North Carolina

  • Wake Forest Baptist Medical Center — Winston-Salem

Ohio

  • The Cleveland Clinic — Cleveland

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2008-03
Est. Completion 2024-12-01
Phase Phase 4

Sponsor

Butler Hospital

58 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00640133

The ClinicalTrials.gov registry entry for NCT00640133 describes a study currently listed as active not recruiting. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Butler Hospital, which has 58 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Obsessive-Compulsive Disorder appearing as the primary indexed condition, and to 2 interventions — of which Sham DBS is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00640133 reports 9 study locations spanning 9 distinct geographic areas — top geographies include California, District of Columbia, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00640133 about?

NCT00640133 is a clinical study titled "Effectiveness of Deep Brain Stimulation for Treating People With Treatment Resistant Obsessive-Compulsive Disorder". This study will evaluate the safety and effectiveness of deep brain stimulation in treating people with severe and otherwise treatment-resistant obsessive-compulsive disorder.

What is the current status of trial NCT00640133?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 27 participants. The study started on 2008-03. Estimated completion is 2024-12-01.

What conditions does trial NCT00640133 study?

This clinical trial studies the following conditions: Obsessive-Compulsive Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00640133?

The interventions under investigation include: Sham DBS (DEVICE), Active DBS (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00640133?

This trial is sponsored by Butler Hospital, which has 58 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00640133 being conducted?

This trial has 9 study locations across California, District of Columbia, Florida, Illinois, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial